Surgical instruments

ABSTRACT

A surgical instrument having an anchor and a plug is capable of anchoring a suture. The suture anchor has an anchor body having a top surface, a bottom surface distal to the top surface, a transverse bore and a well, the well having an outer surface, an inner surface, and an inner bottom surface. The plug has a post, a head, and a bottom face. The anchor body and the anchor plus form a suture anchor. The suture anchor may be used during surgical procedures and can be used in the re-tensioning of a suture.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No.12/102,260, filed on Apr. 14, 2008, which is a continuation-in-part ofU.S. patent application Ser. No. 11/778,951, filed on Jul. 17, 2007,which in turn claims the benefit of U.S. Provisional Applications60/832,035, 60/832,253 and 60/832,289, all of which were filed on Jul.20, 2006, all of which are hereby incorporated by reference, in theirentirety, for any and all purposes.

FIELD

The present disclosure generally related to surgical instruments. Morespecifically, the disclosure relates to a suture anchor.

BACKGROUND

Suture anchors are well known in the art. Suture anchors are typicallyused to anchor soft tissues such as tendons, and the like, to bone usinga suture. The suture anchor is typically secured in a bone and sutures,previously having been inserted into tissue, are then threaded throughthe suture anchor to tension the tissue and hold it in place. The tissueis tensioned to the bone via the suture attached to the anchor.

Typically, the suture is threaded through a small hole, or series ofholes in the anchor and some suture anchors come pre-loaded with thesutures. The suture can then be knotted to prevent release of the suturefrom the suture anchor. However, the need for knotting can increasesurgical time and provide a weak point for suture breakage, hence a needexists for a suture anchor that is fast to use, readily allows forre-tensioning of a suture, and does not introduce knotting weakness tothe suture.

Surgical cannulas are used to enter areas within the body such as theshoulder, knee, or abdomen. The cannula provides a means for passingsurgical instruments into and out of a subject. Cannulas are also usedas a channel to introduce surgical implements such as surgicalinstruments, suture anchors, or sutures. Such surgical cannulastypically have a single chamber that is conducive to instruments oritems touching and either cross-contaminating one another or disturbingthe function of each other. Such surgical cannulas are also subject tothe cannula readily pulling out of the subject or falling into a subjectand requiring re-insertion or extraction. A need exists for cannulasthat resist the tendency to push out of a subject, or fall into asubject. Also multi-chambered cannulas are desired.

SUMMARY

In a first aspect, a surgical instrument is provided comprising (a) ananchor comprising (i) a wall comprising (1) an outer surface havingthreads; and (2) an inner surface; (iii) a first end; and a second end;and (b) a plug comprising a first end, a second end, and an outer wall;wherein the anchor and the plug form a suture anchor capable ofanchoring a suture.

In one embodiment, the outer wall of the plug comprises threads capableof engaging the inner surface of the anchor via a friction fit. Inanother embodiment, the inner surface comprises threads. In anotherembodiment, the outer wall of the plug and the inner wall of the anchoreach have threads capable of engaging each other in a screw-like fashionto secure the plug in the anchor.

In another embodiment, the plug is made of a compressible material. Forexample, the compressible material may be a polymer such as high densitypolyethylene, polyurethane, silicones, or a mixture thereof.

In some embodiments, the first end of the plug has the same diameter asthe second end of the plug. In other embodiments, the first end of theplug has a larger diameter than the second end of the plug, such thatthe plug forms conical shape similar to that of the profile of a funnel.

In another aspect, methods of using a suture anchor is providedcomprising: securing the anchor into a bone, draping a suture through aninterior of the anchor and touching the inner surface; and inserting theplug in the anchor to secure and tension the suture. In someembodiments, the securing is via screwing or cementing of the anchor inthe bone. Other embodiments, further comprise removing the plug;re-tensioning the suture; and replacing the plug in the anchor.

In another aspect, a suture anchor has an anchor body that has a well, atop surface, a bottom surface, and a transverse bore. The well has anouter surface, an inner surface, and an inner bottom surface. In suchembodiments, the anchor and the plug form a suture anchor configured tosecure a surgical suture. In some embodiments, the transverse bore isproximally located to the inner bottom surface. In some embodiments,grooves are formed in the outer surface extending from the transversebore to the top surface. In other embodiments, the outer surface hasrungs and the inner surface has threads. In other embodiments, the postis a threaded post.

In some embodiments, the outer surface has rungs, the inner surface has,the post is a threaded post, and the threads of the inner surface andthe threads of the post are configured to engage in a screw-like fashionto secure the anchor plug in the anchor body.

Methods of using such a suture anchor are also provided. Such methodsinclude boring a nest in a bone; positioning the bottom surface of theanchor body in the nest; threading a suture through the transverse bore;driving the suture anchor into the nest; tensioning the suture; andsecuring the suture in the anchor body with the anchor plug.Alternatively, the threading of the suture precedes the positioning ofthe anchor body in the nest. In some embodiments, the methods alsoinclude loosening or removing the anchor plug, re-tensioning the suture,and tightening or replacing the anchor plug in the anchor body.

In another aspect, surgical instrument is provided comprising (a) acannula comprising a distal end, a proximal end and at least one chamberextending the entire length of the cannula from the proximal end to thedistal end; (b) at least one inflatable donut; and (c) an air passagewayhaving an air inlet; wherein the inflatable donut has a circumference atfull inflation that is greater than a circumference of the cannula. Insome embodiments, the cannula is capable of passing a surgical item intoand out of a subject undergoing surgery. For example, surgical itemsinclude, but are not limited to, surgical instruments, sutures, andimplants.

In some embodiments, the cannula comprises a divider that divides the atleast one chamber extending the entire length of the cannula into atleast two chambers. In some embodiments, the divider is a flexiblediaphragm or divider. In other embodiments, the divider extends the fulllength of the cannula.

In other embodiments, the cannula further comprises a second donut. Insome such embodiments, the second donut is rigid or inflatable. In otherembodiments, the second donut is capable of preventing insertion of thecannula completely into a subject. In yet other embodiments, the seconddonut is formed integrally with the cannula. In yet other embodiments,the second donut is formed separately from the cannula and is attachedto the cannula.

In other embodiments of the cannula, the inflatable donut is capable ofbeing inflated via the air passageway. In some embodiments, a pump isused to inflate the inflatable donut via the air passageway. In otherembodiments, an air-filled syringe inserted through a valve is used toinflate the inflatable donut via the air passageway.

In another aspect, a method of using the cannula is provided comprising:making an incision in the subject at the location in which the cannulais to be inserted; inserting the cannula; and inflating the at least oneinflatable donut. In other embodiments, the method further comprises:conducting a surgical procedure using the cannula; deflating theinflatable donut; and removing the cannula from the subject.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a side view of a suture passer without a suture.

FIG. 2 is a side view of a suture passer having a suture threadedthrough the suture passer.

FIG. 3 is a side view of a suture anchor showing the plug and the nestwith a sutures passing through, prior to insertion of the plug into thenest.

FIG. 4 is a top view of a suture anchor showing the plug and the nestwith a sutures passing through, prior to insertion of the plug into thenest.

FIG. 5 is an illustration of a humerus with a hole bored through aportion for the passage of a suture to secure a rotator cuff bed.

FIG. 6 is an illustration of a humerus with a hole bored through aportion for the passage of a suture to secure a rotator cuff bed.

FIG. 7 is an illustration of a humerus with a hole bored through aportion for the passage of a suture to secure a rotator cuff bed and asuture anchor secured in the humerus.

FIG. 8 is an illustration of a humerus with a hole bored through aportion for the passage of a suture to secure a rotator cuff bed and asuture anchor secured in the humerus with the suture beginning to betensioned.

FIG. 9 is a side view of a cannula.

FIG. 10 is a perspective view of a suture anchor, according to oneembodiment.

FIG. 11 is a perspective view of an anchor body, according to oneembodiment.

FIG. 12 is a perspective view of an anchor plug, according to oneembodiment.

FIG. 13 is a side view of a suture anchor, according to one embodiment.

DESCRIPTION

In one aspect, an instrument comprising a suture passer 100 isdescribed. As shown in FIGS. 1 and 2, the suture passer 100 comprises abody 110 having a tunnel 115, an articulating arm 120, 190 connected tothe body 110 proximally to a first end of the body 110, and a fore end130 distal to the first end of the body 110. In some embodiments, thesuture passer 100, further comprises suture channels 184, 185 throughwhich sutures are threaded to load the suture passer 100. In someembodiments, the suture passer 100 is an arthroscopic instrument. Thesuture passer 100 may be used to grasp tissue and pass a sliding,locking suture in a single grasp of the tissue. The suture passer 100grasps tissue 180 between the body 110 and the articulating arm 120. Thesuture passer 100 then passes a suture loop 140 through the tissue 180.This may be done by loading the suture 140 in a U fashion. A needlepasses through the tunnel 115 then penetrates the tissue 180 passingthrough the suture loop 140. A second needle or a pass of the sameneedle passes through a channel within articulating arm 120 and isdirected through the suture loop 140 and capturing the other end of thesuture. This pulls one end of the suture back in a retrograde fashionthrough the first loop 140 creating a locking stitch. The suture has oneend outside the body 110 and the other end loaded on the other side ofthe suture passer 100. This allows for it to be passed through thesuture loop 140, ultimately forming a locking stitch. One end of thesuture is passed below the tissue 180 and one end is passed above thetissue 180. When the bottom suture is pulled longitudinally it pulls thesuture loop 140 down perpendicular to the tissue 180 resulting inbringing it downward. When the top suture is pulled it brings the tissue180 laterally or in line with the sutures. In one embodiment, thearticulating arm 120 is connected to the body 110 by a joint or a hinge,such that the articulating arm 120 may move relative to the body 110 ina tweezer-like fashion.

In other embodiments, the suture passer 100 will grasp tissue, thusallowing for a loop of a single suture (or multiple sutures) to beplaced from an inferior aspect of the tissue to a superior aspect of thetissue. A needle or grasping agent will then reach through this loop andpull the other end of the suture back through this suture loop. Thiswill create a locking stitch with one end on the superior and one end onthe inferior aspect of the tissue. This is accomplished by a needledriving the loop of suture through the tissue. This needle passesthrough a channel in the inferior arm of the suture passer. The secondneedle or grasping agent penetration runs parallel to the first but onthe other side of the tissue. This needle may be have passage throughthe superior arm of the suture passer. This allows it to be on the otherside of the tissue as the first arm or inferior arm and on the same sideas the suture loop. Thus, going through the loop and pulling back theother end of suture. The result is a locking stitch with suture limbs onboth sides of the tissue.

While conventional suture anchors known to those of skill in the art maybe used to secure sutures required for tissue repair using the suturepasser 100 described above, in another aspect, a suture anchor 300comprising an anchor 310, and a plug 320 is described herein and isillustrated in FIGS. 3-8. Such suture anchors 300 may be used with thesuture passers 100, described above, or the suture anchors 300 may beused in any suturing application known to those of skill in the art.

Suture anchors 300 embodied herein, allow for one or more points offixation of a tissue to be anchored by a single anchor position. Asdescribed below, the suture anchors embodied herein are capable allowingthe tensioning of a tissue with a suture to be adjustable andre-tensionable.

Referring to FIGS. 3-8, the anchor 310 comprises a wall having an outersurface 311, an inner surface 312, that may or may not have threads tosecure the plug 320, a first end 313, and a second end 314. In theeither case of the inner surface 312, having or not having threads, itis a friction fit between the plug 320 and the inner surface 312 thatsecures the plug 320 into the suture anchor 300. In some cases, adiameter of the first end 313 is larger than a diameter of the secondend 314, while in other embodiments, the first end 313 and the secondend 314 have the same diameter. The plug 320 comprises an outer wall 321having threads 325 such that when a suture(s) 330 is draped into theanchor 310 and the plug 320 is inserted into the anchor 310, the plug320 secures the suture(s) 330 via a friction fit between the plug 320and the inner surface 312 of the wall 311. FIGS. 5-8 further illustratethe suture anchor 300 secured in a humerus 510 and with sutures 530anchored in the suture anchor 300.

Anchor 310 may be secured in any bone via a screw mechanism on the outersurface 311 of the wall, or via a cementing of the anchor 310 to thebone, as is known to those of skill in the art. The anchor 310 may alsohave a means for driving the screw mechanism into bone. For example, theanchor 310 may have a hex-head, slot, Phillips-type head, or othershaped head that may be mated to a driver for screwing the anchor 310into bone. Cementing of the anchor 310 to the bone may be accomplishedusing a variety of bone cements known to those of skill in the art. Forexample, curable polymers such as polymethylmethacrylate may be used.

Such suture anchors 300 allow for tightening, adjustment, orre-tensioning of a suture by loosening and/or removal of the plug 320from anchor 310, adjusting or re-tensioning of the suture, andtightening and/or re-insertion of the plug 320 into the anchor 310. Suchsuture anchors 300 also allow for securing of the suture without thetying of knots or replacement of sutures when re-tensioning is required.Suture anchors 300 may be used for the fixation of soft tissue to bone,or of bone to bone.

Suture anchors 300 and plugs 320 may be made from a variety of materialsknown to those of skill in the art. For example, for the suture anchors300 the material is typically a rigid material such as a metal, apolymer, or a ceramic. Biocompatible metals include, but are not limitedto stainless steel, titanium, tantalum, aluminum, chromium, molybdenum,cobalt, silver, and gold, or alloys of such metals that are known tothose of skill in the art. Biocompatible polymers include, but are notlimited to, high-density polyethylenes, polyurethanes, or blends of suchpolymers, as are known to those of skill in the art. Biocompatiblepolymers also include absorbable materials such as polylactic acid,polyglycolic acid, or mixtures thereof. Biocompatible ceramics include,but are not limited to alumina, silica, silicon carbide, siliconnitride, zirconia, and mixtures of any two or more thereof.

The plugs 320 may likewise be prepared from similar metals, polymers,and ceramics, however in some embodiments, the plugs 320 are preparedfrom materials that may be compressed. In such embodiments, the plugmaterial is capable of being compressed from an uncompressed state to acompressed state, prior to or during insertion of the plug 320 into thesuture anchor 300. Such compression allows for the material to recoilfrom the compressed state to the uncompressed state and therebyincreasing the friction fit between the plug 320 and the suture anchor300. Such materials that may be compressed include, but are not limitedto, polyethylenes, silicones, polyesters, polyurethanes, polylacticacid, polyglycolic acid, or mixtures of any two or more thereof.

The anchor 300 may be used to secure sutures tensioning tissue withouttissue to bone direct contact. Examples of such uses of suturetensioning without tissue to bone contact include, but are not limitedto, pelvic surgery, bladder suspension surgery, brow lift or face liftsurgery, hand surgery and the like.

Suture anchors 1000 are also embodied herein, and allow for one or morepoints of fixation of a tissue to be anchored by a single anchorposition. As described below, the suture anchors embodied herein arecapable allowing the tensioning of a tissue with a suture to beadjustable, and re-tensionable.

Referring to FIGS. 10-13, the anchor 1000 comprises an anchor body 1010and a plug 1020. The anchor body 1010 has a central region, or well,that is bored out to accept the anchor plug 1020. The well is surroundedby a wall having an outer surface 1017, an inner surface 1018, and a topsurface 1016. The well also has a bottom inner surface (i.e. the bottomof the well), and a bottom outer surface (i.e. the bottom of the anchorbody 1010). The inner surface 1018 of the anchor body 1010 may havethreads 1015 to accept corresponding threads 1023 on the anchor plug1020. The top edge of the inner surface 1018 of the wall, proximal tothe top surface 1016, may have a bevel 1015. The outer surface 1017 ofthe wall may have rungs or ridges 1014 for securing the plug 1020 inbone or other tissue. The rungs or ridges 1014 provide anchoring abilityto the anchor body 1010 and the suture anchor 1000 as a whole to preventeither from readily pulling out of the bone or other tissue whentensioning a suture, or over the time of implantation in a subject.Alternatively, the bored central region of the anchor body 1010 may notbe threaded, but is a smooth bore that can accept an anchor plug via afriction fit. The anchor body 1010 may accommodate sutures that aredraped into the anchor body 1010, and a friction fit anchor plug is theninserted, or the anchor body 1010 may accommodate sutures that arethreaded through a transverse bore 1012 in the anchor body 1010, to besecured in place by an anchor plug 1020.

The transverse bore 1012 in the anchor body 1010 is capable of receivingone or more sutures to be secured by the suture anchor 1000. Thetransverse bore 1012 is configured proximally to the bottom of the well,such that a suture may be secured between the bottom of the well and abottom face 1026 of the anchor plug 1020. Grooves 1013 are provided thatextend from the transverse bore 1012 to a top surface 1016 of the anchorbody 1010, to allow for movement of a suture through the anchor body1010 when the anchor body 1010 is in place in a bone. Therefore, oncethe anchor body 1010 is driven into a bone or other tissue, with asuture threaded through the transverse bore 1012, the suture is movablein the grooves 1013. The suture may be moved to the desired tension orsecured in the suture anchor 1000 by engaging the anchor plug 1020 inthe anchor body 1010 and driving the anchor plug 1020 until the plugengages the suture, thereby preventing movement of the suture. Thesuture is secured between a bottom face 1026 of the anchor plug 1020 andthe bottom of the well that is formed in the anchor body 1010.

The anchor plug 1020 may have a head 1024, a threaded post 1023 forengaging the threaded inner surface 1018 of the anchor body 1010, and abottom face 1026 that is distal to the head 1024. The anchor plug 1020may also have a bevel 1025 that is complementary to the bevel 1015 ofthe inner surface 1018. When the anchor plug 1020 is fully engaged inthe anchor body 1010, the bevel 1025 is configured to engage the bevel1015 of the inner surface 1018.

The anchor plug 1020 may also be configured to be engaged by acomplementary driving device such that the anchor plug 1020 may betightened or loosened in the anchor body 1010. The head 1024 of theanchor plug 1020 is typically shaped or has a recessed area toaccommodate engagement with a driving device. For example, the anchorplug 1020 may have a hexagonal drive 1021, as shown in FIGS. 10 and 11,or it may have a slotted drive, a Philips drive, a square drive, a stardrive, a nut drive, or other mechanism that is known to those of skillin the art for engaging a complementary drive device. The anchor plug1020 may be configured such that the top of the head 1024 of the anchorplug 1020 is flush with the top surface 1016 of the anchor body 1010,recessed in the anchor body 1010, or above the anchor body 1010, whenthe anchor plug 1020 is fully engaged in the anchor body 1010.

Such suture anchors 1000 allow for tightening, adjustment, orre-tensioning of a suture by tightening, loosening, re-tightening,and/or removing the anchor plug 1020 from anchor body 1010. Such sutureanchors 1000 also allow for securing of the suture without the tying ofknots or replacement of sutures when re-tensioning is required. Sutureanchors 1000 may be used for the fixation of soft tissue to bone, or ofbone to bone.

Suture anchors 1000 and plugs 1020 may be made from a variety ofmaterials known to those of skill in the art. For example, for thesuture anchors 1000 the material is typically a rigid material such as ametal, a polymer, or a ceramic. Biocompatible metals include, but arenot limited to stainless steel, titanium, tantalum, aluminum, chromium,molybdenum, cobalt, silver, and gold, or alloys of such metals that areknown to those of skill in the art. Biocompatible polymers include, butare not limited to, high-density polyethylenes, polyurethanes, or blendsof such polymers, as are known to those of skill in the art.Biocompatible polymers also include absorbable materials such aspolylactic acid, polyglycolic acid, or mixtures thereof. Biocompatibleceramics include, but are not limited to alumina, silica, siliconcarbide, silicon nitride, zirconia, and mixtures of any two or morethereof.

The plugs 1020 may likewise be prepared from similar metals, polymers,and ceramics, however in some embodiments, the anchor plugs are preparedfrom materials that may be compressed. In such embodiments, the plugmaterial is capable of being compressed from an uncompressed state to acompressed state, prior to or during insertion of the plug into theanchor body 1010. Such compression allows for the material to recoilfrom the compressed state to the uncompressed state and therebyincreasing the friction fit between the plug and the anchor body 1010.Such materials that may be compressed include, but are not limited to,polyethylenes, silicones, polyesters, polyurethanes, polylactic acid,polyglycolic acid, or mixtures of any two or more thereof.

The anchor 1000 may be used to secure sutures tensioning tissue withoutdirect contact of tissue to bone. Examples of such uses of suturetensioning without tissue to bone contact include, but are not limitedto, pelvic surgery, bladder suspension surgery, brow lift or face liftsurgery, hand surgery and the like.

Methods of using suture anchors 300, 1000 are also provided. Forexample, referring to FIGS. 5-8 and 10-13, suture anchor 1000 is capableof adjustably retaining a suture. In a typical procedure, a nest, orhole, is drilled into a bone. The anchor body 1010, is then placed atthe top of the nest and inserted such that the transverse bore 1012 isnot obscured in the bone. The suture is then threaded through a tissueto be secured, and the ends of the suture are threaded through thetransverse bore 1012. The anchor body 1010 may then be fully orpartially driven into the nest, such that the suture is guided by thegrooves 1013 and is freely moving through the grooves 1013 andtransverse bore 1012. The anchor plug 1020 may then be engaged in theanchor body 1010 and driven into the anchor body 1010 until sutures arenearly engaged. The tension of the suture may then be set by thesurgeon, or other medical professional, and the anchor plug 1020 fullyengaged to secure the sutures within the suture anchor 1000. Tore-adjust the tension of the suture, the anchor plug 1020 may be drivenin a reverse direction to loosen the anchor plug 1020, thereby allowingfor free movement of the suture and the process of tensioning the suturemay be repeated.

Referring now to FIG. 9, in another aspect, a cannula 900 comprising atleast one chamber 910, 920, an air passage 930 having a valve 940, andat least one inflatable donut 950 is described. The cannula 900 has adistal end 970 and a proximal end 980. The inflatable donut 950 islocated at, or near the distal end 970 of the cannula 900. The cannulamay be used in both arthroscopic and endoscopic surgery. The cannula maybe used to facilitate the passage of surgical items such as but notlimited to instruments, sutures, and implants, into and out of asubject. The cannula 900 may be at least a single chambered passagewayor the cannula 900 may be divided into multiple chambers, such as twochambers 910, 920 as illustrated in FIG. 9, or more than two chambers,depending upon the intended use of the cannula for a given procedure orprocedures. In some embodiments, a flexible diaphragm is used to dividecannula 900 into multiple chambers 910, 920. In some such embodiments,the flexible diaphragm extends the entire length of the cannula 900. Thedonut 950 is an inflatable donut that, when inflated, has a largerdiameter than a diameter of the cannula 900. Cannula 900 may alsocomprise a second donut 960, that may be rigid or inflatable. The seconddonut 960 may be located at or near the proximal end 980. In one aspect,the cannula 900 is inserted through the skin of a subject and the donut950 is inflated via the air passage 930. In one embodiment, inflation ofdonut 950 is via a pump connected to the valve 940, and subsequentfilling of the air chamber 930 and donut 950 with air from the pump. Inanother embodiment, inflation of donut 950 is via insertion of anair-filled syringe through the valve 940, and subsequent filling of theair chamber 930 and donut 950 with air from the syringe. The valve 940may comprise rubber(s), silicone(s), or other materials known to thoseof skill in the art to be useful for the insertion and removal ofsyringes or other devices that may be used for inflation of donut 950.Other methods of inflating the donut 950 will be readily apparent tothose of skill in the art. Inflation of donut 950 prevents inadvertentremoval of the cannula from the subject during surgical procedures. Thepresence of inflatable donut 950 allows for less trauma to an insertionpoint in the skin of a subject by allowing for a cannula 900 of smalldiameter to be inserted, but then the larger diameter donut 950 preventsremoval. In embodiments where the second donut 960 is present, thesecond donut 960 prevents the inadvertent full insertion of the cannulainto a subject beyond the surface of the skin of the subject. As notedabove, because the second donut 960 does not pass through the skin of asubject, the second donut may be made of a rigid material or the seconddonut 960 may be inflatable. The second donut 960 may be integrallyformed with cannula 900 or it may be formed separately and attached tocannula 900. In embodiments, where both the first donut 950 and thesecond donut 960 are inflatable, the donuts 950, 960 may besimultaneously inflatable in a “dumbbell” formation allowing for theinflation both within, via the first donut 950, and external, 960, tothe body together.

Generally, cannulas are used to enter areas within the body such as theshoulder, knee or abdomen. Cannulas are also used as a channel tointroduce surgical implements such as surgical instruments, sutureanchors, or sutures. The cannulas embodied herein allow for separatechambers which allow multiple instruments or items to be entered intothe joint but partitioned from one another. Another feature is anexpandable, inflatable device on the end of the cannula which preventsexpulsion of the cannula from the cavity as intracavitary pressureincreases. The inflatable device, i.e. inflatable donut, locks thecannula in place.

In another aspect, methods for using instruments described herein, areprovided. For example in some embodiments, methods are disclosed forusing the suture passer 100, suture anchor 300, and cannula 900 aredescribed. The embodied methods allow for tissue repair. In someembodiments, the methods provided allow for arthroscopic rotator cuffrepair, by attempting to recreate the true native footprint of therotator cuff of a subject. In some embodiments, such methods comprisepreparing the rotator cuff bed, boring a tunnel 510 (FIGS. 5-8), orhole, through a portion of bone such as a humerus 520, passing a suture530 through the tunnel 510, suturing the tissue using a suture passer100, and anchoring the sutures 530 in the suture anchor 300, therebysecuring the rotator cuff muscles to the bone

In some embodiments of the methods, the suture passer 100 descendsthrough one chamber 950, 960 of the cannula 900, grasping tissue. Thesuture passer 100 passes a locking stitch as described above, followedby removal of the suture passer 100, with the sutures remaining in thechamber 950, 960 of the cannula 900. The other chamber 950, 960 of thecannula 900 has a humerus drill inserted. A small hole is bored in agreater tuberosity. One limb of a suture is then passed through thebone. A suture anchor 300 is then placed into the greater tuberosity.Sutures may be placed through the suture anchor 300 either before orafter insertion. If not previously completed, the suture anchor 300 isthen fixated in the bone. The sutures are then tensioned thus tensioningthe tissue. The plug 320 of the suture anchor 300 is then engaged in theanchor 310 and locked into position, thus securing the sutures. Thisstep can be repeated to alter the tension of the sutures and thereforere-tensioning the sutures and tissue.

For the purposes of this disclosure and unless otherwise specified, “a”or “an” means “one or more.”

One skilled in the art will readily realize that all ranges discussedcan and do necessarily also describe all subranges therein for allpurposes, and that all such subranges also form part and parcel of thisinvention. Any listed range can be easily recognized as sufficientlydescribing and enabling the same range being broken down into at leastequal halves, thirds, quarters, fifths, tenths, etc. As a non-limitingexample, each range discussed herein can be readily broken down into alower third, middle third and upper third, etc.

While some embodiments have been illustrated and described, it should beunderstood that changes and modifications can be made therein inaccordance with ordinary skill in the art without departing from theinvention in its broader aspects as defined in the following claims.

1. A suture anchor comprising: an anchor body comprising: a wellcomprising: an outer surface; an inner surface; and an inner bottomsurface; a top surface; a bottom surface distal to the top surface; anda transverse bore; an anchor plug comprising: a post; a head; and abottom face; wherein the anchor body and the anchor plug form a sutureanchor configured to secure a suture.
 2. The suture anchor of claim 1,wherein the transverse bore is proximal to the inner bottom surface. 3.The suture anchor of claim 1, further comprising grooves in the outersurface extending from the transverse bore to the top surface.
 4. Thesuture anchor of claim 1, the outer surface comprising rungs and theinner surface comprising threads.
 5. The suture anchor of claim 1,wherein the post is a threaded post.
 6. The suture anchor of claim 1,the outer surface comprising rungs, the inner surface comprisingthreads, and wherein the post is a threaded post, and the threads of theinner surface and the threads of the post are configured to engage tosecure the anchor plug in the anchor body.
 7. The suture anchor of claim1, wherein a region between the top surface of the anchor body and theinner surface of the well is a bevel surface of the anchor body.
 8. Thesuture anchor of claim 7, wherein the anchor plug further comprises abevel surface on a bottom face of the head.
 9. The suture of anchor ofclaim 8, wherein the bevel surface of the head and the bevel of theanchor body are configured to engage one another when the anchor plug isfully engaged in the anchor body.